The management of non-culprit vessel(s) in patients with unstable angina/non-ST elevation myocardial infarction and chronic kidney dysfunction

被引:2
|
作者
Liao, Guang-zhi [1 ]
Li, Yi-ming [1 ]
Liu, Ting [1 ]
Bai, Lin [1 ]
Chen, Xue-feng [1 ]
Ye, Yu-yang [1 ]
Chai, Hua [2 ]
Peng, Yong [1 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Cardiol, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, West China Sch Med, Dept Acad Affairs, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Cardiol, 37 Guoxue St, Chengdu 610041, Peoples R China
关键词
UA; NSTEMI; chronic kidney dysfunction; multivessel disease; percutaneous coronary intervention; multivessel interventions; CORONARY-ARTERY-DISEASE; GLOMERULAR-FILTRATION-RATE; REVASCULARIZATION STRATEGIES; RANDOMIZED-TRIAL; MULTIVESSEL; INTERVENTION; ASSOCIATION; LESION; RISK;
D O I
10.1111/imj.16201
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and AimsThe clinical effects of multivessel interventions in patients with unstable angina/non-ST-segment elevation myocardial infarction (UA/NSTEMI), multivessel disease (MVD) and chronic kidney disease (CKD) remain uncertain. This study aimed to investigate the safety and effectiveness of intervention in non-culprit lession(s) among this cohort. MethodsWe consecutively included patients diagnosed with UA/NSTEMI, MVD and CKD between January 2008 and December 2018 at our centre. After successful percutaneous coronary intervention (PCI), we compared 48-month overall mortality between those undergoing multivessel PCI (MV-PCI) through a single-procedure or staged-procedure approach and culprit vessel-only PCI (CV-PCI) after 1:1 propensity score matching. We conducted stratified analyses and tests for interaction to investigate the modifying effects of critical covariates. Additionally, we recorded the incidence of contrast-induced nephropathy (CIN) to assess the perioperative safety of the two treatment strategies. ResultsOf the 749 eligible patients, 271 pairs were successfully matched. Those undergoing MV-PCI had reduced all-cause mortality (hazard ratio (HR): 0.67, 95% confidence interval (CI): 0.48-0.67). Subgroup analysis showed that those with advanced CKD (estimated glomerular filtration rate (eGFR) & LE; 30 mL/min/1.73 m(2)) could not benefit from MV-PCI (P = 0.250), and the survival advantage also tended to diminish in diabetes (P (interaction) < 0.01; HR = 0.95, 95% CI = 0.65-1.45). Although the staged-procedure approach (N = 157) failed to bring additional survival benefits compared to single-procedure MV-PCI (N = 290) (P = 0.460), it showed a tendency to decrease the death risk. CIN risks in MV-PCI and CV-PCI groups were not significantly different (risk ratio = 1.60, 95% CI = 0.94-2.73). ConclusionAmong patients with UA/NSTEMI and non-diabetic CKD and an eGFR > 30 mL/min/1.73 m(2), MV-PCI was associated with a reduced risk of long-term death but did not increase the incidence of CIN during the management of MVD compared to CV-PCI. And staged procedures might be a preferable option over single-procedure MV-PCI.
引用
收藏
页码:473 / 482
页数:10
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